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Genome wide association study of clinical duration and age at onset of sporadic CJD

Genome wide association study of clinical duration and age at onset of sporadic CJD

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a8105e366d44473aa02be9676f81d759

Publication information

Publisher

Public Library of Science (PLoS)

More information

Scope and Contents

Contents

Human prion diseases are rare, transmissible and often rapidly progressive dementias. The most common type, sporadic Creutzfeldt-Jakob disease (sCJD), is highly variable in clinical duration and age at onset. Genetic determinants of late onset or slower progression might suggest new targets for research and therapeutics. We assembled and array geno...

Alternative Titles

Full title

Genome wide association study of clinical duration and age at onset of sporadic CJD

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_a8105e366d44473aa02be9676f81d759

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a8105e366d44473aa02be9676f81d759

Other Identifiers

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0304528

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